Fibre reactive azo dyes

ABSTRACT

The present invention refers to dyestuffs of the formula I  
                 
 
     wherein  
     each of R 1 , R 2 , R 3 , R 4  and R 5 , independently, is H or an optionally substituted alkyl group;  
     each of X 1  and X 2 , independently, is a labile atom or group;  
     each of x and y, independently, is 0 or 1 and at least one of x and y is 1;  
     each of a and b is 2 to 5 and when each of x and y is 1, a&gt;b; and  
     z is 0, 1, 2, 3 or 4; and  
     wherein the variables D 1  and D 2  are defined as given in claim 1, processes for their preparation and their use for dyeing and printing hydroxy- and/or carboxamido-containing fiber materials.

[0001] The present invention relates to the field of fibre-reactive dyes.

[0002] Dyestuffs containing chromophores linked via a piperazine type linking unit are known from literature and are described for example in EP-A-0126265, EP-A-0693538, WO99/05224 and WO00/08104.

[0003] The inventor of the present invention has surprisingly found that dyestuffs with very strong and economic shades exhibiting excellent fastness properties can be obtained if piperazine type linking units are used to link two chromophores each selected from a specific range of chromophores as defined below.

[0004] The present invention claims dyestuffs of the formula I

[0005] wherein

[0006] each of R¹, R², R³, R⁴ and R⁵, independently, is H or an optionally substituted alkyl group;

[0007] each of X₁ and X₂, independently, is a labile atom or group;

[0008] each of x and y, independently, is 0 or 1 and at least one of x and y is 1;

[0009] each of a and b is 2 to 5 and when each of x and y is 1, a>b; and

[0010] z is 0, 1, 2, 3 or 4;

[0011] D, is a group of the formula II

[0012]  wherein

[0013] B is H or SO₃M;

[0014] M is H, an alkali metal, an ammonium ion or the equivalent of an alkaline earth metal;

[0015] * indicates the bond to the triazinylamino group;

[0016] Ar₁ is a group of the formula III or of the formula IV

[0017]  wherein

[0018] the or each Y independently is SO₃M or an alkyl group, c is 0, 1 or 2, M is defined as given above and # indicates the bond to the azo group; or

[0019] D₁ is a group of the formula IIa

[0020]  wherein

[0021] B is H or SO₃M;

[0022] M is H, an alkali metal, an ammonium ion or the equivalent of an alkaline earth metal;

[0023] * indicates the bond to the triazinylamino group;

[0024] Ar₄ is a group of the formula IIIa or of the formula IVa

[0025]  wherein

[0026] Y² is —N═N—Ar₅, M is defined as given above and # indicates the bond to the azo group, wherein

[0027] Ar₅ is a group of the formula IIIb or of the formula IVb

[0028]  wherein the or each Y³ independently is SO₃M or an alkyl group, d is 0, 1 or 2, M is defined as given above and # indicates the bond to the azo group; or

[0029] D₁ is a group of the formula V

[0030]  wherein

[0031] M, * and Ar₁ are defined as given above; or

[0032] D₁ is a group of the formula VI

[0033]  wherein

[0034] * is defined as given above

[0035] n is 0, 1, 2 or 3;

[0036] the or each R₆ independently is H, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, NHCONH₂, NHCO(C₁-C₄)-alkyl, SO₃M or halogen;

[0037] Ar₂ is a group of the formula VII or of the formula VIII

[0038]  wherein

[0039] the or each Y¹ independently is SO₃M or an alkyl group or —N═N—Ar₃, wherein Ar₃ is an optionally substituted phenylene or naphthylene moiety;

[0040] c is 0, 1 or 2, M is defined as given above and # indicates the bond to the azo group; or

[0041] D₁ is a group of the formula XV

[0042]  wherein R⁶, Ar₁, n and * are defined as given above; or

[0043] D₁ is an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore;

[0044] D₂ is a group of the formula II, provided D₁ is not a group of the formula V; or

[0045] D₂ is a group of the formula IIa; or

[0046] D₂ is a group of the formula IX

[0047]  wherein

[0048] A and E are independently OH or NH₂ and A≠E;

[0049] G is H, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, SO₃M or halogen; and

[0050] Ar₁, M and * are defined as given above; or

[0051] D₂ is a group of the formula VI; or

[0052] D₂ is a group of the formula X

[0053]  wherein M and * are defined as given above; or

[0054] D₂ is a group of the formula XI

[0055]  wherein M and * are defined as given above; or

[0056] D₂ is a group of the formula XII

[0057]  wherein

[0058] R⁷ is H or (C₁-C₄)-alkyl;

[0059] L is a divalent moiety and

[0060] M and * are defined as given above; or

[0061] D₂ is a group of the formula XIII

[0062]  wherein

[0063] R⁸ and R⁹, independently, are H, halogen, (C₁-C₄)-alkyl or (C₁-C₄)-alkoxy;

[0064] and M, Ar₁ and * are defined as given above; or

[0065] D₂ is a group of the formula XIV

[0066]  wherein

[0067] M′ is a metal atom;

[0068] Pc is a phthalocyanine chromophore;

[0069] e is <4; and

[0070] M, L and R⁷ are defined as given above; or

[0071] D₂ is a group of the formula XV; or

[0072] D₂ is an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore.

[0073] Alkyl groups may be straight-chain or branched and are preferably (C₁-C₄)-alkyl groups, for example methyl, ethyl, n-propyl, i-propyl or n-butyl. Substituted alkyl groups are preferably substituted by hydroxyl, (C₁-C₄)-alkoxy, halogen or carboxyl groups.

[0074] The same logic applies for alkoxy groups, which are thus preferably (C₁-C₄)-alkoxy groups and particularly methoxy and ethoxy.

[0075] Substituted phenylene or naphthylene moieties standing for Ar₃ are preferably of the formulae III and IV above.

[0076] A divalent moiety L occurring in the groups of the formulae XII and XIV is preferably a phenylene or (C₁-C₆)-alkylene, preferably (C₁-C₄)-alkylene moiety. The phenylene moiety is optionally substituted by (SO₃M)_(f), where f=0, 1, or 2 and (R₁₆)_(g), where R₁₆ is (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy or halogen.

[0077] R¹ to R⁵ are preferably H or methyl. R³, R⁴ and R⁵ are especially preferably H.

[0078] X₁ and X₂ are preferably halogen like fluorine and chlorine or optionally substituted pyridinium like 3- and 4-carboxypyridinium. X₁ and X₂ are especially preferably chlorine.

[0079] M is preferably H, an alkaline metal, like sodium, potassium and lithium and is especially preferably sodium.

[0080] M′ is preferably Cu, Ni or Al.

[0081] An azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore standing for D₁ or D₂ is preferably an optionally metallized monoazo chromophore of the formulae (XVIa) or (XVIb)

K—N═N—O-*  (XVIa)

*-K—N═N—O  (XVIb)

[0082] wherein

[0083] * indicates the bond to the triazinylamino group in formula I; and

[0084] one of K and O is an acetoacetamidoaryl group wherein the aryl moiety is optionally substituted and wherein the azo linkage in the formulae XVIa and XVIb is linked to the methylene group of the acetoacetamidoaryl group; an optionally substituted pyridonly group; an optionally substituted pyrazolonyl group or an optionally substituted pyrimidinyl group;

[0085] and the other of K and O is a phenyl or napthyl group which is unsubstituted or substituted by one to four substituents selected from the group consisting of (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, H₂NCONH, CH₃CONH, NHCO(C₁-C₄), hydroxyl, amino, cyano, (C₁-C₄)-alkyl-amino, halogen, COOM, SO₃M, aminophenyl, aminonaphthyl, (C₁-C₄)-alky-aminophenyl, (C₁-C₄)-alkyl-aminonaphthyl, amidophenyl, amidonaphthyl, sulphonamidophenyl and sulfonamidonaphthyl, wherein M is defined as given above.

[0086] An acetoacetamidoaryl group can be substituted in its aryl moiety preferably by (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, halogen, H₂NCONH, CH₃CONH or SO₃M, wherein M is defined as given above.

[0087] Preferred acetoacetamidoaryl groups are of the formulae XVII and XVIII

[0088] wherein

[0089] R¹⁰ is H or (C₁-C₄)-alkyl;

[0090] P is an optionally substituted aryl group;

[0091] # indicates the bond to the azo group of the monoazo chromophore of formulae (XVIa) and (XVIb); and

[0092] * indicates the bond to the triazinylamino group of the dyestuff of formula I.

[0093] P is preferably phenyl or naphthyl which is optionally substituted by (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, halogen, nitro, H₂NCONH, CH₃CONH or SO₃M, wherein M is defined as given above.

[0094] An optionally substituted pyridonyl group is preferably of the formulae (XIX) or (XX)

[0095] wherein

[0096] R¹² is H, (C₁-C₄)-alkyl or phenyl;

[0097] R¹³ is H, (C₁-C₄)-alkyl, CN, CONH₂ or CH₂SO₃M, wherein M is defined as given above;

[0098] R¹⁴ is (C₁-C₄)-alkyl or phenyl;

[0099] q is zero or is 1-4;

[0100] # indicates the bond to the azo group of the monoazo chromophore of formulae (XVIa) and (XVIb); and

[0101] * indicates the bond to the triazinylamino group of the dyestuff of the formula I.

[0102] An optionally substituted pyrazolonyl group is preferably of the formulae (XXI) or

[0103] wherein

[0104] R¹⁵ is methyl, carboxyl or methoxycarbonyl;

[0105] X is OH or NH₂;

[0106] the or each R¹¹, independently, is (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, halogen, H₂NCONH, CH₃CONH or SO₃M, wherein M is defined as given above;

[0107] r is zero or 1-4, preferably zero or 1-3, still more preferably 0, 1 or 2, especially 1 or 2;

[0108] # indicates the bond to the azo group of the monoazo chromophore of formulae (XVIa) and (XVIb); and

[0109] * indicates the bond to the triazinylamino group of the dyestuff of the formula I.

[0110] An optionally substituted pyrimidinyl group is preferably of the formula (XXIII)

[0111] wherein each of S, T and U, independently, is H, (C₁-C₄)-alkoxy, hydroxy, (C₁-C₄)-alkylthio, mercapto, amino, (C₁-C₄)-alkyl-amino or di-(C₁-C₄)-alkyl-amino; and # indicates the bond to the azo group of the monoazo chromophore of formulae (XVIa) and (XVIb).

[0112] Preferred dyestuffs of the formula (I) are bright orange dyestuffs, wherein D₁ and D₂ both are a group of formula (II), with the proviso, however, that D₁≠D₂ or D₁=D₂ if R¹≠R².

[0113] In still more preferred bright orange dyestuffs of the formula (I)

[0114] X₁ and X₂ are both chlorine;

[0115] R³, R⁴ and R⁵ are H;

[0116] a=b=2 with x=0 and y=1 or x=1 and y=0; and

[0117] D₁ and D₂ are both a group of the formula (IIa)

[0118] wherein B and M are defined as given above,

[0119] In especially preferred bright orange dyestuffs of the formula (I)

[0120] D₁ is a group of the formula (IIb)

[0121] and D₂ is a group of formula (IIc)

[0122] or D₁ and D₂ are both a group of formula (IIc) and R¹≠R², especially one of R¹ and R² is H and the other methyl.

[0123] Especially preferred bright orange dyestuffs of the formula (I) are of the formulae (Ia) and (Ib)

[0124] wherein

[0125] B is SO₃M and R¹ is H or B is H and R¹ is methyl and M is defined as given above.

[0126] Further preferred dyestuffs of the formula (I) are homogeneous black dyestuffs, wherein

[0127] D₁ is a group of the formula (II) and

[0128] D₂ is a group of the formula (IX).

[0129] In still more preferred homogeneous black dyestuffs of the formula (I)

[0130] X₁ and X₂ are both chlorine;

[0131] R³, R⁴ and R⁵ are H;

[0132] a=b=2 with x=0 and y=1 or x=1 and y=0;

[0133] D₁ is a group of the formula (IIa)

[0134]  wherein B and M are defined as given above; and

[0135] D₂ is a group of the formula (IXa)

[0136]  wherein A is OH and E is NH₂ or A is NH₂ and E is OH and Ar₁ and M are defined as given above. A is especially preferred NH₂ and E is OH.

[0137] Especially preferred homogeneous black dyestuffs of the formula (I) are of the formulae (Ic) and (Id)

[0138] wherein M is defined as given above.

[0139] Further preferred dyestuffs of the formula (I) are dull red dyestuffs, wherein

[0140] D₁ is a group of the formula (V) and

[0141] D₂ is a group of the formula (XV).

[0142] In still more preferred dull red dyestuffs of the formula (I)

[0143] X₁ and X₂ are both chlorine;

[0144] R³, R⁴ and R⁵ are H;

[0145] a=b=2 with x=0 and y=1 or x=1 and y=0;

[0146] D₁ is a group of the formula (Va)

[0147]  wherein Ar₁, M and * are defined as given above; and

[0148] D₂ is a group of the formula (XVa)

[0149]  wherein

[0150] R₆′ is H, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy or halogen;

[0151] R₆″ is H, NHCONH₂, NHCO(C₁-C₄)-alkyl or SO₃M; and

[0152] Y, c and M are defined as given above.

[0153] Especially preferred dull red dyestuffs of the formula (I) are of the formula (Ie)

[0154] wherein

[0155] a is 1 and b is 0 or a is 0 and b is 1;

[0156] Ar₁′ is 2-sulphophenyl, 2,5-disulphophenyl, 1-sulpho-2-naphthyl or 1,5-disulpho-2-naphthyl and

[0157] Ar₁″ is 4,8-disulpho-2-naphthyl or 3,6,8-trisulpho-2-naphthyl.

[0158] Further preferred dyestuffs of the formula (I) are homogeneous green dyestuffs, wherein

[0159] D₁ is a group of the formula (XV) or an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore; and

[0160] D₂ is a group of the formula (IX), a group of the formula (X), a group of the formula (XI), a group of the formula (XII), a group of the formula (XIII) or a group of the formula (XIV).

[0161] In still more preferred homogeneous green dyestuffs of the formula (I)

[0162] X₁ and X₂ are both chlorine;

[0163] R³, R⁴ and R⁵ are H; and

[0164] a=b=2 with x=0 and y=1 or x=1 and y=0.

[0165] Further preferred dyestuffs of the formula (I) are yellow dyestuffs, wherein

[0166] D₁ is a group of the formula (II), a group of the formula (VI) or an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore; and

[0167] D₂ is a group of the formula (VI), or an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore.

[0168] In still more preferred homogeneous green dyestuffs of the formula (I)

[0169] X₁ and X₂ are both chlorine;

[0170] R³, R⁴ and R⁵ are H; and

[0171] a=b=2 with x=0 and y=1 or x=1 and y=0.

[0172] The dyestuffs of the present invention can be present as a preparation in solid or liquid (dissolved) form. In solid form they generally contain the electrolyte salts customary in the case of water-soluble and in particular fibre-reactive dyes, such as sodium chloride, potassium chloride and sodium sulfate, and also the auxiliaries customary in commercial dyes, such as buffer substances capable of establishing a pH in aqueous solution between 3 and 7, such as sodium acetate, sodium borate, sodium bicarbonate, sodium citrate, sodium dihydrogen-phosphate and disodium hydrogenphosphate, small amounts of siccatives or, if they are present in liquid, aqueous solution (including the presence of thickeners of the type customary in print pastes), substances which ensure the permanence of these preparations, for example mold preventatives.

[0173] In general, the dyestuffs of the present invention are present as dye powders containing 10 to 80% by weight, based on the dye powder or preparation, of a strength-standardizing colorless diluent electrolyte salt, such as those mentioned above. These dye powders may additionally include the aforementioned buffer substances in a total amount of up to 10%, based on the dye powder. If the dye mixtures of the present invention are present in aqueous solution, the total dye content of these aqueous solutions is up to about 50% by weight, for example between 5 and 50% by weight, and the electrolyte salt content of these aqueous solutions will preferably be below 10% by weight, based on the aqueous solutions. The aqueous solutions (liquid preparations) may include the aforementioned buffer substances in an amount which is generally up to 10% by weight, for example 0.1 to 10% by weight, preference being given to up to 4% by weight, especially 2 to 4% by weight.

[0174] A dyestuff of the formula I may for example be prepared by reacting a piperazine compound of the formula XXIII

[0175] wherein R³, R⁴, R⁵, a, b, x, y, and z are defined as given above, with a compound of the formula XXIV

[0176] wherein R², X₂ and D₂ are defined as given above and X₃ is a labile atom or a group capable of reaction with an amine, preferably chlorine, and with a compound of the formula XXV

[0177] wherein R¹, X₁ and D₁ are defined as given above and X₄ has one of the meanings of X₃.

[0178] It is possible to react a compound of formula XXIII first with a compound of the formula XXIV to form a compound of the formula XXVI

[0179] wherein all variables are defined as given above,

[0180] which is then reacted with a compound of the formula XXV to a dyestuff of the formula I.

[0181] As an alternative is it also possible to react a compound of the formula XXIII first with a compound of the formula XXV to form the compound of the formula XXVII

[0182] wherein all variables are defined as given above,

[0183] which is then reacted with a compound of the formula XXIV to a dyestuff of the formula I.

[0184] In general, one mole of a compound of the formula XXIII is reacted with 1 mole of a compound of the formula XXIV and 1 mole of a compound of the formula XXV in a manner known per se to a skilled person.

[0185] The compounds of the formulae XXIII, XXIV and XXV are known or can easily be prepared by a skilled person using methods which are known per se. As an example, a compound of the formula XXIV, wherein X₂ is chlorine can be obtained by reacting cyanuric chloride with a compound of the formula XXVIII

[0186] wherein R² and D₂ are defined as given above.

[0187] The compounds of the formula XXVIII can be prepared by means of customary diazotization and coupling reactions in a manner familiar to those skilled in the art.

[0188] The dyestuffs of the instant invention are reactive dyestuffs suitable for dyeing and printing hydroxy- and/or carboxamido-containing fibre materials by the application and fixing methods numerously described in the art for fibre-reactive dyes. They provide exceptionally bright, exceptionally strong and economic shades. Such dyes especially when used for exhaust dyeing of cellulosic materials can exhibit excellent properties including build-up, aqueous solubility, light-fastness, wash off and robustness to process variables. They are also wholly compatible with similar dyes designed for high temperature (80-100° C.) application to cellulosic textiles, and thus lead to highly reproducible application processes, with short application times.

[0189] The present invention therefore also provides for use of the inventive dyestuffs for dyeing and printing hydroxy- and/or carboxamido-containing fibre materials and processes for dyeing and printing such materials using a dyestuff according to the invention. Usually the dyestuff is applied to the substrate in dissolved form and fixed on the fibre by the action of an alkali or by heating or both.

[0190] Hydroxy-containing materials are natural or synthetic hydroxy-containing materials, for example cellulose fiber materials, including in the form of paper, or their regenerated products and polyvinyl alcohols. Cellulose fiber materials are preferably cotton but also other natural vegetable fibers, such as linen, hemp, jute and ramie fibres. Regenerated cellulose fibers are for example staple viscose and filament viscose.

[0191] Carboxamido-containing materials are for example synthetic and natural polyamides and polyurethanes, in particular in the form of fibers, for example wool and other animal hairs, silk, leather, nylon-6,6, nylon-6, nylon-11, and nylon-4.

[0192] Application of the inventive dyestuffs is by generally known processes for dyeing and printing fiber materials by the known application techniques for fibre-reactive dyes. The dyestuffs according to the invention are highly compatible with similar dyes designed for high temperature (80-100° C.) applications and are advantageously useful in exhaust dyeing processes.

[0193] Similarly, the conventional printing processes for cellulose fibers, which can either be carried out in single-phase, for example by printing with a print paste containing sodium bicarbonate or some other acid-binding agent and the colorant, and subsequent steaming at appropriate temperatures, or in two phases, for example by printing with a neutral or weakly acid print paste containing the colorant and subsequent fixation either by passing the printed material through a hot electrolyte-containing alkaline bath or by overpadding with an alkaline electrolyte-containing padding liquor and subsequent batching of this treated material or subsequent steaming or subsequent treatment with dry heat, produce strong prints with well defined contours and a clear white ground. Changing fixing conditions has only little effect on the outcome of the prints. Not only in dyeing but also in printing the degrees of fixation obtained with dye mixtures of the invention are very high. The hot air used in dry heat fixing by the customary thermofix processes has a temperature of from 120 to 200° C. In addition to the customary steam at from 101 to 103° C., it is also possible to use superheated steam and high pressure steam at up to 160° C.

[0194] The inventive dyestuffs can in addition be used to produce inks useful for printing the substrates described above, for example textiles, especially cellulosic textiles, and paper. Such inks can be used in all technologies, for example conventional printing, ink-jet printing or bubble-jet printing (for information on such printing technologies see for example Text. Chem. Color, Volume 19(8), pages 23 ff and Volume 21, pages 27 ff).

[0195] Acid-binding agents responsible for fixing the dyes to cellulose fibers are for example water-soluble basic salts of alkali metals and of alkaline earth metals of inorganic or organic acids, and compounds which release alkali when hot. Of particular suitability are the alkali metal hydroxides and alkali metal salts of weak to medium inorganic or organic acids, the preferred alkali metal compounds being the sodium and potassium compounds. These acid-binding agents are for example sodium hydroxide, potassium hydroxide, sodium carbonate, sodium bicarbonate, potassium carbonate, sodium formate, sodium dihydrogen-phosphate and disodium hydrogenphosphate.

[0196] Treating the dyestuffs according to the invention with the acid-binding agents with or without heating bonds the dyes chemically to the cellulose fibers. Especially the dyeings on cellulose, after they have been given the usual aftertreatment of rinsing to remove unfixed dye portions, show excellent properties.

[0197] The dyeings of polyurethane and polyamide fibers are customarily carried out from an acid medium. The dyebath may contain for example acetic acid and/or ammonium sulfate and/or acetic acid and ammonium acetate or sodium acetate to bring it to the desired pH. To obtain a dyeing of acceptable levelness it is advisable to add customary leveling auxiliaries, for example based on a reaction product of cyanuric chloride with three times the molar amount of an aminobenzenesulfonic acid or aminonaphthalenesulfonic acid or based on a reaction product of for example stearylamine with ethylene oxide. In general the material to be dyed is introduced into the bath at a temperature of about 40° C. and agitated therein for some time, the dyebath is then adjusted to the desired weakly acid, preferably weakly acetic acid, pH, and the actual dyeing is carried out at temperature between 60 and 98° C. However, the dyeings can also be carried out at the boil or at temperatures up to 120° C. (under superatmospheric pressure).

EXAMPLE 1

[0198] 1-(2-aminoethyl) piperazine (2.6 g, 0.02 mol) was added dropwise to a stirred suspension of the orange dichlorotriazinyl dye (3) (0.02 mol) in water (400 mls) at ambient temperature and pH6. The pH was then adjusted to 10 with sodium carbonate solution and maintained at this pH for 20 minutes, yielding a solution of the orange dye (5). To this solution was added the orange dichlorotriazinyl dye (4) (0.02 mol) and the solution was maintained at pH 10 and ambient temperature for 48 hours. The pH was adjusted to 6 with 2N HCl and the dye precipitated by the addition of NaCl. The precipitated dye was filtered off, salt removed by dialysis and dried to give the expected dye (1) (16.0 g). (λ_(max)=491 nm, ε=65500, ν_(1/2)=115 nm). Other analytical data were in full agreement with the expected structure.

EXAMPLES 2-4

[0199] Following exactly analogous procedures as described in Example 1 the following dyes were synthesised.

Example Dye 1 Dye 2 λ max/nm 2 a c 495 3 a b 493 4 b a 491

EXAMPLE 5

[0200] 1-(2-aminoethyl) piperazine (1.4 g, 0.011 mol) was added dropwise to a stirred suspension of the orange dichlorotriazinyl dye (7) (0.011 mol) in water (400 mls) at ambient temperature and pH6. The pH was then adjusted to 10 with sodium carbonate solution and maintained at this pH for 20 minutes, yielding a slurry of the orange dye (8). To this slurry was added the navy dichlorotriazinyl dye (9) (0.011 mol) and the solution was maintained at pH 10 and ambient temperature for 24 hours. The pH was adjusted to 6 with 2N HCl and the dye precipitated by the addition of methylated spirits. The precipitated dye was filtered off, and dried to give the expected dye (6) (18.0 g). (λ_(max)=623 nm, ε=42500, ν_(1/2)=115 nm). Other analytical data were in full agreement with the expected structure.

EXAMPLES 6-11

[0201] Following exactly analogous procedures as described in Example 5 the following dyes were synthesised.

Example Dye 1 Dye 2 λ max/nm 6 c f 614 7 c e 619 8 a f 613 9 C h 618 10 A h 622 11 A d 608

EXAMPLE 12

[0202] 1-(2-aminoethyl) piperazine (1.0 g, 0.0077 mol) was added dropwise to a stirred suspension of the red dichlorotriazinyl dye (11) (0.0077 mol) in water (300 mls) at ambient temperature and pH6. The pH was then adjusted to 10 with sodium carbonate solution and maintained at this pH for 20 minutes, yielding the red dye (12). To this solution was added the yellow dichlorotriazinyl dye (13) (0.0077 mol) and the solution was maintained at pH 10 and ambient temperature for 24 hours. The pH was adjusted to 6 with 2N HCl and the dye precipitated by the addition of methylated spirits. The precipitated dye was filtered off, and dried to give the expected dye (10) (10.6 g). (λ_(max)=516 nm, ε=46000, ν_(1/2)=115 nm). Other analytical data were in full agreement with the expected structure.

[0203] precipitated by the addition of methylated spirits. The precipitated dye was filtered off, and dried to give the expected dye (10) (10.6 g). (λ_(max)=516 nm, ε=46000, ν_(1/2)=115 nm). Other analytical data were in full agreement with the expected structure.

EXAMPLES 13-27

[0204] Following exactly analogous procedures as described in Example 12 the following dyes were synthesised.

Example Dye 1 Dye 2 λ max/nm 13 i l 462 14 l i 561 15 i n 518 16 n i 522 17 l j 520 18 j n 514 19 n j 515 20 m l 436 21 l m 467 22 m n 507 23 n m 507 24 k l 504 25 l k 473 26 k n 506 27 n k 499

EXAMPLE 28

[0205] 1-(2-aminoethyl) piperazine (0.32 g, 0.0025 mol) was added dropwise to a stirred suspension of the yellow dichlorotriazinyl dye (15) (0.0025 mol) in water (200 mls) at ambient temperature and pH6. The pH was then adjusted to 10 with sodium carbonate solution and maintained at this pH for 20 minutes, yielding the yellow dye (16). To this slurry was added the navy dichlorotriazinyl dye (17) (0.0025 mol) and the solution was maintained at pH 10 and ambient temperature for 4 hours. The pH was adjusted to 6 with 2N HCl and the dye precipitated by the addition of methylated spirits. The precipitated dye was filtered off, and dried to give the expected dye (14) (4.9 g). (λ_(max)=(415 nm) and 614 nm, ε=36800, ν_(1/2)=117 nm). Other analytical data were in full agreement with the expected structure.

EXAMPLES 29-38

[0206] Following exactly analogous procedures as described in Example 28 the following dyes were synthesised.

Example Dye 1 Dye 2 λ max/nm 29 l u 420, 626 30 p v 416, 616 31 l t 440, 622 32 p t 426, 622 33 q s 451, 619 34 p s 426, 623 35 r s 620 36 l w 454, 601 37 q w 452, 599 38 p w 416, 636

EXAMPLE 39

[0207] 1-(2-aminoethyl) piperazine (2.6 g, 0.02 mol) was added dropwise to a stirred suspension of the orange dichlorotriazinyl dye (19) (0.02 mol) in water (400 mls) at ambient temperature and pH6. The pH was then adjusted to 10 with sodium carbonate solution and maintained at this pH for 20 minutes, yielding a solution of the orange dye (20). To this solution was added the yellow dichlorotriazinyl dye (21) (0.02 mol) and the solution was maintained at pH 10 and ambient temperature for 48 hours. The pH was adjusted to 6 with 2N HCl and the dye precipitated by the addition of NaCl. The precipitated dye was filtered off, salt removed by dialysis and dried to give the expected dye (18) (16.0 g). (λ_(max)=485 nm, ε=46000, ν_(1/2)=115 nm). Other analytical data were in full agreement with the expected structure.

EXAMPLES 40-56

[0208] Following exactly analogous procedures as described in Example 39 the following dyes were synthesised.

Example Dye 1 Dye 2 λ max/nm 40 b x 458 41 b y 472 42 c y 468 43 a x 449 44 c x 457 45 a y 458 46 a p 481 47 a r 483 48 a l 483 49 n p 435 50 c n 485 51 n c 486 52 n l 441 53 l n 444 54 p r 416 55 l r 416 56 l p 424

[0209] The dyes of the following Examples 57-95 can be synthezised by one of the methods given above.

EXAMPLE 57

[0210]

[0211] λmax=489 and 617 nm

EXAMPLE 58

[0212]

[0213] λmax=429

EXAMPLE 59

[0214]

[0215] λmax=414.5

EXAMPLE 60

[0216]

[0217] λmax=431

EXAMPLE 61

[0218]

[0219] λmax=430

EXAMPLE 62

[0220]

[0221] λmax=473

EXAMPLE 63

[0222]

[0223] λmax=423

EXAMPLE 64

[0224]

[0225] λmax=431

EXAMPLE 65

[0226]

[0227] λmax=416

EXAMPLE 66

[0228]

[0229] λmax=475

EXAMPLE 67

[0230]

[0231] λmax=470

EXAMPLE 68

[0232]

[0233] λmax=472

EXAMPLE 69

[0234]

[0235] λmax=489

EXAMPLE 70

[0236]

[0237] λmax=476

EXAMPLE 71

[0238]

[0239] λmax=492

EXAMPLE 72

[0240]

[0241] λmax=484

EXAMPLE 73

[0242]

[0243] λmax=479

EXAMPLE 74

[0244]

[0245] λmax=480

EXAMPLE 75

[0246]

[0247] λmax=511

EXAMPLE 76

[0248]

[0249] λmax=420

EXAMPLE 77

[0250]

[0251] λmax=425

EXAMPLE 78

[0252]

[0253] λmax=507

EXAMPLE 79

[0254]

[0255] λmax=439

EXAMPLE 80

[0256]

[0257] λmax=478

EXAMPLE 81

[0258]

[0259] λmax=508

EXAMPLE 82

[0260]

[0261] λmax=516

EXAMPLE 83

[0262]

[0263] λmax=506

EXAMPLE 84

[0264]

[0265] λmax=426

EXAMPLE 85

[0266]

[0267] λmax=443

EXAMPLE 86

[0268]

[0269] λmax 421

EXAMPLE 87

[0270]

[0271] λmax=449

EXAMPLE 88

[0272]

[0273] λmax=501

EXAMPLE 89

[0274]

[0275] λmax=514

EXAMPLE 90

[0276]

[0277] λmax=509

EXAMPLE 91

[0278]

[0279] λmax=495

EXAMPLE 92

[0280]

[0281] λmax=459

EXAMPLE 93

[0282]

[0283] λmax=511

EXAMPLE 94

[0284]

[0285] λmax=459

EXAMPLE 95

[0286]

[0287] λmax=512 

1. A dyestuff of the formula I

wherein each of R¹, R², R³, R⁴ and R⁵, independently, is H or an optionally substituted alkyl group; each of X₁ and X₂, independently, is a labile atom or group; each of x and y, independently, is 0 or 1 and at least one of x and y is 1; each of a and b is 2 to 5 and when each of x and y is 1, a>b; and z is 0, 1, 2, 3 or
 4. D₁ is a group of the formula II

 wherein B is H or SO₃M; M is H, an alkali metal, an ammonium ion or the equivalent of an alkaline earth metal; indicates the bond to the triazinylamino group; Ar₁ is a group of the formula III or of the formula IV

 wherein the or each Y independently is SO₃M or an alkyl group, c is 0, 1 or 2, M is defined as given above and # indicates the bond to the azo group; or D₁ is a group of the formula IIa

 wherein B is H or SO₃M; M is H, an alkali metal, an ammonium ion or the equivalent of an alkaline earth metal; indicates the bond to the triazinylamino group; Ar₄ is a group of the formula IIIa or of the formula IVa

 wherein Y² is —N═N—Ar₅, M is defined as given above and # indicates the bond to the azo group, wherein Ar₅ is a group of the formula IIIb or of the formula IVb

 wherein the or each Y³ independently is SO₃M or an alkyl group, d is 0, 1 or 2, M is defined as given above and # indicates the bond to the azo group; or D₁ is a group of the formula V

 wherein M, * and Ar₁ are defined as given above; or D₁ is a group of the formula VI

 wherein * is defined as given above n is 0, 1, 2 or 3; the or each R₆ independently is H, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, NHCONH₂, NHCO(C₁-C₄)-alkyl, SO₃M or halogen; Ar₂ is a group of the formula VII or of the formula VIII

 wherein the or each Y¹ independently is SO₃M or an alkyl group or —N═N—Ar₃₁ wherein Ar₃ is an optionally substituted phenylene or naphthylene moiety; c is 0, 1 or 2, M is defined as given above and # indicates the bond to the azo group; or D₁ is a group of the formula (XV)

 wherein R⁶, Ar₁, n and * are defined as given above D₁ is an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore; D₂ is a group of the formula II, provided D₁ is not a group of the formula V; or D₂ is a group of the formula IIa; or D₂ is a group of the formula IX

 wherein A and E are independently OH or NH₂ and A≠E; G is H, (C₁-C₄)-alkyl, (C₁-C₄)-alkoxy, SO₃M or halogen; and Ar₁, M and * are defined as given above; or D₂ is a group of the formula VI; or D₂ is a group of the formula X

 wherein M and * are defined as given above; or D₂ is a group of the formula XI

 wherein M and * are defined as given above; or D₂ is a group of the formula XII

 wherein R⁷ is H or (C₁-C₄)-alkyl; L is a divalent moiety and M and * are defined as given above; or D₂ is a group of the formula XIII

 wherein R⁸ and R⁹, independently, are H, halogen, (C₁-C₄)-alkyl or (C₁-C₄)-alkoxy; and M, Ar₁ and * are defined as given above; or D₂ is a group of the formula XIV

 wherein M′ is a metal atom; Pc is a phthalocyanine chromophore; e is <4; and M, L and R⁷ are defined as given above; or D₂ is a group of the formula XV; or D₂ is an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore.
 2. A dyestuff of the formula I as claimed in claim 1, wherein D₁ and D₂ both are a group of the formula (II), with the proviso, however, that D₁≠D₂ or D₁=D₂ if R¹≠R².
 3. A dyestuff of the formula I as claimed in claim 1, wherein D₁ is a group of the formula (II) and D₂ is a group of the formula (IX).
 4. A dyestuff of the formula I as claimed in claim 1, wherein D₁ is a group of the formula (V) and D₂ is a group of the formula (XV).
 5. A dyestuff of the formula I as claimed in claim 1, wherein D₁ is a group of the formula (XV) or an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore; and D₂ is a group of the formula (IX), a group of the formula (X), a group of the formula (XI), a group of the formula (XII), a group of the formula (XIII) or a group of the formula (XIV).
 6. A dyestuff of the formula I as claimed in claim 1, wherein D₁ is a group of the formula (II), a group of the formula (VI) or an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore; and is D₂ is a group of the formula (VI), or an azoacetoacetamidoaryl, azopyridone, azopyrazolone or an azopyrimidine chromophore.
 7. A dyestuff as claimed in one or more of claims 1 to 6, wherein X₁ and X₂ are halogen, preferably chlorine.
 8. A dyestuff as claimed in one or more of claims 1 to 7, wherein M is H or an alkaline metal, preferably sodium. 9 A dyestuff as claimed in one or more of claims 1 to 8, wherein R³, R⁴ and R⁵ are H.
 10. A dyestuff as claimed in one or more of claims 1 to 9, wherein a=b=2 with x=0 and y=1 or x=1 and y=0.
 11. A process for preparing a dyestuff of formula I as claimed in one or more of claims 1 to 10 by reacting a piperazine compound of the formula XXIII

wherein R³, R⁴, R⁵, a, b, x, y, and z are defined as given in claim 1, with a compound of the formula XXIV

wherein R², X₂ and D₂ are defined as given in claim 1 and X₃ is a labile atom or a group capable of reaction with an amine, preferably chlorine, and with a compound of the formula XXV

wherein R¹, X₁ and D₁ are defined as given in claim 1 and X₄ has one of the meanings of X₃.
 12. A process for dyeing and printing hydroxy- and/or carboxamido-containing fibre materials in which a dyestuff of the formula I according to one or more of claims 1 to 10 is used. 